CN1021345C - 以总碱值高、粘度低的ii族金属的高碱性硫化烷基酚盐为活性组分的润滑油组合物 - Google Patents
以总碱值高、粘度低的ii族金属的高碱性硫化烷基酚盐为活性组分的润滑油组合物 Download PDFInfo
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- CN1021345C CN1021345C CN87105448A CN87105448A CN1021345C CN 1021345 C CN1021345 C CN 1021345C CN 87105448 A CN87105448 A CN 87105448A CN 87105448 A CN87105448 A CN 87105448A CN 1021345 C CN1021345 C CN 1021345C
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- Prior art keywords
- family metal
- alkyl
- gram
- calcium
- weight
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- 229910052751 metal Inorganic materials 0.000 title claims description 110
- 239000002184 metal Substances 0.000 title claims description 110
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- 239000000314 lubricant Substances 0.000 title claims description 15
- 239000000470 constituent Substances 0.000 title description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 83
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- 239000011575 calcium Substances 0.000 claims description 60
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- 229910052791 calcium Inorganic materials 0.000 claims description 56
- -1 hydrocarbyl sulfonate Chemical compound 0.000 claims description 52
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- 239000004480 active ingredient Substances 0.000 claims description 25
- 239000011777 magnesium Substances 0.000 claims description 10
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- 229910052788 barium Inorganic materials 0.000 claims description 8
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 8
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 24
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 15
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
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- 229910021518 metal oxyhydroxide Inorganic materials 0.000 description 6
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
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- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 6
- 239000003643 water by type Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- JNVCSEDACVAATK-UHFFFAOYSA-L [Ca+2].[S-]SSS[S-] Chemical compound [Ca+2].[S-]SSS[S-] JNVCSEDACVAATK-UHFFFAOYSA-L 0.000 description 5
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- BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 4
- YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 description 4
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- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- ZFXVRMSLJDYJCH-UHFFFAOYSA-N calcium magnesium Chemical compound [Mg].[Ca] ZFXVRMSLJDYJCH-UHFFFAOYSA-N 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 239000000385 dialysis solution Substances 0.000 description 1
- HIKZOIYUQFYFBB-UHFFFAOYSA-N didodecyl decanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCCCCCC HIKZOIYUQFYFBB-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000021050 feed intake Nutrition 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 239000005414 inactive ingredient Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- YZKRIHZCXGPZGB-UHFFFAOYSA-L zinc;oxido-propan-2-yloxy-propan-2-ylsulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound [Zn+2].CC(C)OP([O-])(=S)SC(C)C.CC(C)OP([O-])(=S)SC(C)C YZKRIHZCXGPZGB-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89459986A | 1986-08-08 | 1986-08-08 | |
| US894,599 | 1986-08-08 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN87105448A CN87105448A (zh) | 1988-04-13 |
| CN1021345C true CN1021345C (zh) | 1993-06-23 |
Family
ID=25403296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN87105448A Expired - Fee Related CN1021345C (zh) | 1986-08-08 | 1987-08-08 | 以总碱值高、粘度低的ii族金属的高碱性硫化烷基酚盐为活性组分的润滑油组合物 |
Country Status (15)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5391310A (en) * | 1993-11-23 | 1995-02-21 | Cincinnati Milacron Inc. | Sulfurized aqueous machining fluid composition |
| JP3454593B2 (ja) * | 1994-12-27 | 2003-10-06 | 旭電化工業株式会社 | 潤滑油組成物 |
| US7405185B2 (en) | 2003-09-26 | 2008-07-29 | Chevron Oronite Company Llc | Process for making Group II metal overbased sulfurized alkylphenols |
| ES2655116T3 (es) * | 2006-09-19 | 2018-02-16 | Infineum International Limited | Una composición de aceite lubricante |
| US8933002B2 (en) * | 2011-11-10 | 2015-01-13 | Chevron Oronite Company Llc | Lubricating oil compositions |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3178368A (en) * | 1962-05-15 | 1965-04-13 | California Research Corp | Process for basic sulfurized metal phenates |
| NL134001C (enrdf_load_stackoverflow) * | 1965-10-29 | |||
| US3367867A (en) * | 1966-01-04 | 1968-02-06 | Chevron Res | Low-foaming overbased phenates |
| US3424679A (en) * | 1966-08-15 | 1969-01-28 | Chevron Res | Nonvicinal glycols in overbased phenate preparation |
| GB1144084A (en) * | 1966-08-24 | 1969-03-05 | Orobis Ltd | Improvements in or relating to lubricant additives |
| US3464970A (en) * | 1967-03-13 | 1969-09-02 | Maruzen Oil Co Ltd | Process for preparing over-based sulfurized calcium phenates |
| GB1280749A (en) * | 1970-06-18 | 1972-07-05 | Maruzen Oil Company Ltd | Process for preparation of over-based sulphurized phenates |
| US3801507A (en) * | 1972-08-18 | 1974-04-02 | Chevron Res | Sulfurized metal phenates |
| GB1429243A (en) * | 1973-02-22 | 1976-03-24 | Orobis Ltd | Overbased phenates |
| GB1551819A (en) * | 1975-05-23 | 1979-09-05 | Exxon Research Engineering Co | Production of basic magnesium detergent additives |
| US4104180A (en) * | 1975-05-23 | 1978-08-01 | Exxon Research & Engineering Co. | Production of overbased metal phenates |
| JPS5476604A (en) * | 1977-11-11 | 1979-06-19 | Orobis Ltd | Preparation of dispersing cleaner and lubricant composition containing same |
| DE3379663D1 (en) * | 1982-05-14 | 1989-05-24 | Exxon Research Engineering Co | Lubricating oil additives |
| FR2529226B1 (fr) * | 1982-06-24 | 1987-01-16 | Orogil | Procede de preparation d'alkylphenates sulfurises de metaux alcalino-terreux utilisables comme additifs pour huiles lubrifiantes |
| FR2549080B1 (fr) * | 1983-07-11 | 1986-04-04 | Orogil | Procede de preparation d'additifs detergents-dispersants de tres haute alcalinite a base de calcium et additifs detergents-dispersants pour huiles lubrifiantes ainsi obtenus |
| FR2587353B1 (fr) * | 1985-09-17 | 1987-11-20 | Orogil | Nouveaux additifs detergents-dispersants suralcalinises stables a l'hydrolyse pour huiles lubrifiantes et leur procede de preparation |
-
1987
- 1987-07-20 NZ NZ221128A patent/NZ221128A/xx unknown
- 1987-07-28 CA CA000543119A patent/CA1341002C/en not_active Expired - Fee Related
- 1987-07-31 ZA ZA875686A patent/ZA875686B/xx unknown
- 1987-07-31 AU AU76334/87A patent/AU602343B2/en not_active Ceased
- 1987-08-06 DK DK410087A patent/DK410087A/da not_active Application Discontinuation
- 1987-08-07 ES ES87307025T patent/ES2054677T3/es not_active Expired - Lifetime
- 1987-08-07 MX MX026955A patent/MX168483B/es unknown
- 1987-08-07 KR KR1019870008668A patent/KR880002818A/ko not_active Ceased
- 1987-08-07 BR BR8704053A patent/BR8704053A/pt not_active Application Discontinuation
- 1987-08-07 JP JP62197989A patent/JPS6346297A/ja active Pending
- 1987-08-07 DE DE3785807T patent/DE3785807T3/de not_active Expired - Fee Related
- 1987-08-07 NO NO873316A patent/NO167659C/no unknown
- 1987-08-07 EP EP87307025A patent/EP0259974B2/en not_active Expired - Lifetime
- 1987-08-08 CN CN87105448A patent/CN1021345C/zh not_active Expired - Fee Related
-
1988
- 1988-01-05 IN IN05/MAS/88A patent/IN170575B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IN170575B (enrdf_load_stackoverflow) | 1992-04-11 |
| AU602343B2 (en) | 1990-10-11 |
| EP0259974A3 (en) | 1988-08-10 |
| DK410087D0 (da) | 1987-08-06 |
| NO873316L (no) | 1988-02-09 |
| KR880002818A (ko) | 1988-05-11 |
| DE3785807T2 (de) | 1993-10-07 |
| CA1341002C (en) | 2000-05-30 |
| CN87105448A (zh) | 1988-04-13 |
| ZA875686B (en) | 1988-04-27 |
| EP0259974B1 (en) | 1993-05-12 |
| DE3785807T3 (de) | 1997-06-12 |
| ES2054677T3 (es) | 1994-08-16 |
| NZ221128A (en) | 1989-09-27 |
| NO167659B (no) | 1991-08-19 |
| AU7633487A (en) | 1988-02-11 |
| EP0259974B2 (en) | 1997-03-26 |
| EP0259974A2 (en) | 1988-03-16 |
| NO873316D0 (no) | 1987-08-07 |
| NO167659C (no) | 1991-11-27 |
| MX168483B (es) | 1993-05-26 |
| BR8704053A (pt) | 1988-04-05 |
| DE3785807D1 (de) | 1993-06-17 |
| JPS6346297A (ja) | 1988-02-27 |
| DK410087A (da) | 1988-02-09 |
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| C14 | Grant of patent or utility model | ||
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| C19 | Lapse of patent right due to non-payment of the annual fee | ||
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